Canonical Allele Identifier: CA343774771
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879056G>T (hg19) chr1:g.173909918G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909918G>T , CM000663.2:g.173909918G>T GRCh38
NC_000001.10:g.173879056G>T , CM000663.1:g.173879056G>T GRCh37
NC_000001.9:g.172145679G>T NCBI36
NG_012462.1:g.12461C>A , LRG_577:g.12461C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.787C>A MANE Select ENSP00000356671.3:p.Pro263Thr
ENST00000367698.3:c.787C>A ENSP00000356671.3:p.Pro263Thr
ENST00000487183.1:n.438C>A
ENST00000617423.4:c.559+1946C>A ENSP00000478688.1:n.559+1946C>A
NM_000488.3:c.787C>A , LRG_577t1:c.787C>A NP_000479.1:p.Pro263Thr
XM_005245198.2:c.643C>A XP_005245255.1:p.Pro215Thr
NM_001365052.1:c.643C>A NP_001351981.1:p.Pro215Thr
NM_000488.4:c.787C>A MANE Select NP_000479.1:p.Pro263Thr
NM_001365052.2:c.643C>A NP_001351981.1:p.Pro215Thr
NM_001386302.1:c.910C>A NP_001373231.1:p.Pro304Thr
NM_001386303.1:c.868C>A NP_001373232.1:p.Pro290Thr
NM_001386304.1:c.766C>A NP_001373233.1:p.Pro256Thr
NM_001386305.1:c.763-33C>A NP_001373234.1:n.763-33C>A
NM_001386306.1:c.571C>A NP_001373235.1:p.Pro191Thr
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